Multimodal Luminescence in Antimony(III)-Doped Hybrid Manganese(II)-Based Compounds for Dynamic Anticounterfeiting Encryption and Optical Thermometry
The synergistic interaction between Mn2+ and Sb3+ ions in organic–inorganic hybrid single crystals has unlocked exciting optical applications for multiple band emission centers. Here, (TPMP)2MnBr4:Sb3+ single crystals were synthesized. They exhibited energy transfer from Mn2+ to Sb3+ ions, producing color-tunable luminescence and multiband emission. The dual emission leveraged d-d transitions in Mn2+ for green emission and self-trapped excitons in Sb3+ for broad red emission. Precise control of the excitation energy created broad color gamut modulation on the CIE chromaticity diagram, ranging across green, yellow, and red. Furthermore, there were distinct temperature sensitivities of the Mn2+ and Sb3+ emission centers, leading to robust fluorescence intensity ratios for temperature sensing with high relative sensitivity (3.92% K–1) and absolute sensitivity (5.42% K–1). These results indicated significant (TPMP)2MnBr4:Sb3+ potential for optical temperature sensing and dynamic information for anticounterfeiting encryption. This work provides a pathway for energy-transfer dynamics and luminescence applications of Mn2+-Sb3+ systems.
Authors
- Henan Li
- Xiangyan Yun (ORCID: https://orcid.org/0009-0005-3245-2540)
- Yumeng Shi (ORCID: https://orcid.org/0000-0002-9623-3778)
- Hanlin Hu (ORCID: https://orcid.org/0000-0001-5617-0998)
- Yujie Xie (ORCID: https://orcid.org/0000-0002-2260-9242)
- Yukang Lu
Institutions
- Shenzhen University (CN)
- Shenzhen Polytechnic University (CN)
- Beijing Jiaotong University (CN)
- Integrated Optoelectronics (Norway) (NO)
- Physical Sciences (United States) (US)
- Department of Physics, Mathematics and Informatics (BY)
- The Polytechnic University of Japan (JP)
Publication Details
- Journal
- Chemistry of Materials
- Published
- 2025-09-09
- DOI
- https://doi.org/10.1021/acs.chemmater.5c01141
- Primary Topic
- Luminescence and Fluorescent Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00